Dengue Fever Clinical Trial
Official title:
A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Safety, Pharmacokinetic, Pharmacodynamic and Preliminary Efficacy Study of IC14 in Adult Patients With Dengue Fever
Randomized, double-blind, placebo-controlled, safety, PK/PD and preliminary efficacy study of intravenous IC14 in adult patients in a dengue-endemic region presenting with fever > 38°C for < 48 hours with a positive NS1 strip assay or reverse-transcriptase polymerase chain reaction assay for dengue virus.
The study will be conducted in two parts and will include an open label phase of a single
dose of IC14 (Part A) and a randomized phase of multiple doses of IC14 and placebo (Part B).
Up to 52 patients will be enrolled in both parts of the study.
Part A will consist of 12 patients given one of three doses of IC14 as a single dose
open-label . Each patient must complete 14 days before the enrollment of subsequent patients.
Part A subjects will be hospitalized for 4 days. During and at the end of 4-day admission to
the clinical research unit, and on Study Days 5, 6, 7, 14, 21 and 32, Part A patients will
have their health status assessed. The last subject in Part A must complete 32 days of
participation before Part B of the trial is opened.
Part B consists of 40 patients randomized equally to one of 4 dosing regimens which will
include a single dose or multiple doses of IC14 or placebo given at different dosing
frequencies. In Part B, Cohort 1 and 2 subjects (single dose) will be inpatient for 4 days
and Cohort 3 and 4 subjects (four daily doses) will be inpatient for 5 days. During and at
the end of the admission to the clinical research unit, and on Study Days 5, 6, 7, 14, 21 and
32, Part B patients will have their health status assessed.
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